Canonical Allele Identifier: CA2466845280
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956869_154956871delinsCTA , CM000685.2:g.154956869_154956871delinsCTA GRCh38
NC_000023.10:g.154185144_154185146delinsCTA , CM000685.1:g.154185144_154185146delinsCTA GRCh37
NC_000023.9:g.153838338_153838340delinsCTA NCBI36
NG_011403.1:g.70853_70855delinsTAG
NG_011403.2:g.70853_70855delinsTAG

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1752+86_1752+88delinsTAG MANE Select ENSP00000353393.4:n.1752+86_1752+88delins...
ENST00000647125.1:c.*1628+86_*1628+88delinsTAG ENSP00000496062.1:n.*1628+86_*1628+88deli...
ENST00000360256.8:c.1752+86_1752+88delinsTAG ENSP00000353393.4:n.1752+86_1752+88delins...
NM_000132.3:c.1752+86_1752+88delinsTAG NP_000123.1:n.1752+86_1752+88delinsTAG
XM_011531126.1:c.1647+86_1647+88delinsTAG XP_011529428.1:n.1647+86_1647+88delinsTAG...
NM_000132.4:c.1752+86_1752+88delinsTAG MANE Select NP_000123.1:n.1752+86_1752+88delinsTAG
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